Analyte Monitoring System Having an Alert

ABSTRACT

Described herein are analyte monitoring systems including a receiver or data processing component that is configured to automatically issue a first alert notification when a first predetermined number of consecutive data packets are not received from the sensor/sensor electronics, and automatically issue a second alert notification when a second predetermined number of consecutive data packets are not received by the sensor/sensor electronics. The receiver may also be configured to enable a user to disenable alert or alarm notifications that are triggered based on detected events.

RELATED APPLICATIONS

The present application is a continuation of U.S. patent applicationSer. No. 14/928,359 filed Oct. 30, 2015, now U.S. patent Ser. No.10/009,244, which is a continuation of U.S. patent application Ser. No.14/262,700 filed Apr. 25, 2014, now U.S. Pat. No. 9,178,752, which is acontinuation of U.S. patent application Ser. No. 13/953,356 filed Jul.29, 2013, now U.S. Pat. No. 8,730,058, which is a continuation of U.S.patent application Ser. No. 12/761,387 filed Apr. 15, 2010, now U.S.Pat. No. 8,497,777, which claims priority under 35 U.S.C. § 119(e) toU.S. Provisional Patent Application No. 61/169,654, entitled “AnalyteMonitoring System with Alert for Missed Data packet”, filed on Apr. 15,2009 and U.S. Provisional Patent Application No. 61/169,652, entitled“Analyte Monitoring System with Muted Alarm Capability”, filed on Apr.15, 2009, the disclosures of each of which are incorporated herein byreference in their entirety for all purposes.

BACKGROUND

Diabetes Mellitus is an incurable chronic disease in which the body doesnot produce or properly utilize insulin. Insulin is a hormone producedby the pancreas that regulates blood glucose. In particular, when bloodglucose levels rise, e.g., after a meal, insulin lowers the bloodglucose levels by facilitating blood glucose to move from the blood intothe body cells. Thus, when the pancreas does not produce sufficientinsulin (a condition known as Type 1 Diabetes) or does not properlyutilize insulin (a condition known as Type II Diabetes), the bloodglucose remains in the blood resulting in hyperglycemia or abnormallyhigh blood sugar levels.

People suffering from diabetes often experience long-term complications.Some of these complications include blindness, kidney failure, and nervedamage. Additionally, diabetes is a factor in acceleratingcardiovascular diseases such as atherosclerosis (hardening of thearteries), which often leads to stroke, coronary heart disease, andother diseases, which can be life threatening.

The severity of the complications caused by both persistent high glucoselevels and blood glucose level fluctuations has provided the impetus todevelop diabetes management systems and treatment plans. In this regard,diabetes management plans historically included multiple daily testingof blood glucose levels typically by a finger-stick to draw and testblood. The disadvantage with finger-stick management of diabetes is thatthe user becomes aware of his blood glucose level only when he performsthe finger-stick. Thus, blood glucose trends and blood glucose snapshotsover a period of time is unknowable.

More recently, diabetes management has included the implementation ofglucose monitoring systems. Glucose monitoring systems have thecapability to continuously monitor a user's blood glucose levels. Thus,such systems have the ability to illustrate not only present bloodglucose levels but a snapshot of blood glucose levels and blood glucosefluctuations over a period of time. Further, when monitoring the bloodglucose levels, the glucose monitoring systems have the capability tooutput an alert notification to notify the user of an event, such as ahyperglycemic or hypoglycemic event. Although the alert features are abig advantage to managing diabetes, sometimes an alert, such as the loudsounding of an audible alarm, can occur at an inopportune time.

Additionally, the accuracy of continuous glucose monitoring systemsdepend on the proper and prompt relay of data information about minuteto minute glucose levels from a sensor to a receiver component of thesystem. When the data information fails to reach the receiver, the lackof glucose data can not only affect the displayed glucose readings tothe user, but also provide the user with a false sense of security.

Therefore, a need exists for a user to have the capability toselectively disenable and re-enable alert notification features of aglucose monitoring system for a predetermined period of time and for theanalyte monitoring system to sound an alarm or otherwise alert the userto missed data packets so that the user can intervene.

SUMMARY

Embodiments of the present disclosure include analyte monitoring systemsincluding a receiver or data processing component configured toautomatically issue a first alert notification when a firstpredetermined number of consecutive data packets are not received fromthe sensor/sensor electronics, and automatically issue a second alertnotification when a second predetermined number of consecutive datapackets are not received by the sensor/sensor electronics. The receivermay be configured to enable a user to disenable alert or alarmnotifications that are triggered based on detected events.

In certain embodiments, the receiver has the capability of displayingblood glucose readings related to the received data. The receiver isalso configured to output an alert notification based on an event, suchas, for example, a hypoglycemic event, a hyperglycemic event, animpending hypoglycemic event, an impending hypoglycemic event, or when apredetermined number of consecutive data packets are not received by thereceiver. Additionally, the receiver is configured to provide a user thecapability to selectively disenable the alarm for a predetermined timeperiod and also re-enable the alarm prior to elapse of the predeterminedtime period.

In certain embodiments, the alert can be a visual alert, such as adisplayed icon, an audible alert, such as a beep or music, a tactilealert such as a vibration of a system component or a combinationthereof. The alert can have multiple modes of notification. In oneembodiment, the alert is tri-modal. Thus, the alert can simultaneouslyinclude an audible, visual, and tactile notification. In this regard,the receiver can be configured to mute only one or two of the threealarm modes. For the purpose of illustration and not limitation, theaudible notification can be muted by the user while the tactile (e.g.,vibration) and visual (e.g., icon) notifications are not disenabled.Thus, when an event triggers the alert notification, the user isnotified of the event or condition by feeling the vibration and/orseeing the icon.

As explained in greater detail below, the alert notification, orcomponents thereof, can be selectively disenabled for a predeterminedamount of time up to a maximum predetermined period of time, such as,for example, twelve hours. In this regard, the receiver can beconfigured to allow the user to select disenabling the alarm for anentire predetermined period (e.g., two hours, six hours) oralternatively, the selective disenablement of the alarm for thepredetermined period can be set in one-hour increments or less.

Embodiments further include a receiver that may be configured such thatthe alert is incapable of being disenabled for a critical event such asa low glucose level, a decreasing blood glucose trend, a hypoglycemicevent, or a blood glucose level above or below a particular thresholdlevel. In this regard, the receiver is capable of allowing a user todisenable the alarm only for non-critical events, such as but notlimited to, battery status, sensor life, and the like.

INCORPORATION BY REFERENCE

The following patents, applications and/or publications are incorporatedherein by reference for all purposes: U.S. Pat. Nos. 4,545,382;4,711,245; 5,262,305; 5,264,104; 5,320,715; 5,509,410; 5,543,326;5,593,852; 5,601,435; 5,628,890; 5,820,551; 5,822,715; 5,899,855;5,918,603; 6,071,391; 6,103,033; 6,120,676; 6,121,009; 6,134,461;6,143,164; 6,144,837; 6,161,095; 6,175,752; 6,270,455; 6,284,478;6,299,757; 6,338,790; 6,377,894; 6,461,496; 6,503,381; 6,514,460;6,514,718; 6,540,891; 6,560,471; 6,579,690; 6,591,125; 6,592,745;6,600,997; 6,605,200; 6,605,201; 6,616,819; 6,618,934; 6,650,471;6,654,625; 6,676,816; 6,730,200; 6,736,957; 6,746,582; 6,749,740;6,764,581; 6,773,671; 6,881,551; 6,893,545; 6,932,892; 6,932,894;6,942,518; 7,167,818; and 7,299,082; U.S. Published Application Nos.2004/0186365, now U.S. Pat. No. 7,811,231; 2005/0182306, now U.S. Pat.No. 8,771,183; 2007/0056858, now U.S. Pat. No. 8,298,389; 2007/0068807,now U.S. Pat. No. 7,846,311; 2007/0227911, now U.S. Pat. No. 7,887,682;2007/0233013; 2008/0081977, now U.S. Pat. No. 7,618,369; 2008/0161666;and 2009/0054748, now U.S. Pat. No. 7,885,698; U.S. patent applicationSer. Nos. 12/131,012; 12/242,823, now U.S. Pat. No. 8,219,173; Ser. No.12/363,712, now U.S. Pat. No. 8,346,335; Ser. Nos. 12/495,709;12/698,124; 12/699,653; 12/699,844, now U.S. Pat. No. 8,930,203; andSer. No. 12/714,439 and U.S. Provisional Application Nos. 61/230,686 and61/227,967.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 illustrates a block diagram of an analyte monitoring system forpracticing one or more embodiments of the present disclosure;

FIG. 2 is a flowchart illustrating a method for detecting a missed datapacket and issuing an alert in accordance with one embodiment of thepresent disclosure;

FIG. 3 is a flowchart illustrating a concurrent passive notificationroutine in a receiver of the analyte monitoring system in accordancewith one embodiment of the present disclosure;

FIG. 4 is a flowchart illustrating an alarm notification disenabling andre-enabling routine in a receiver of the analyte monitoring system inaccordance with one embodiment of the present disclosure; and

FIG. 5 is a flowchart illustrating a method for detecting an alertcondition in accordance with one embodiment of the present disclosure.

DETAILED DESCRIPTION

Reference will now be made in detail to the embodiments of the presentdisclosure, examples of which are illustrated in the accompanyingfigures. As such, various aspects will be described in conjunction withthe detailed description of the device. However, there is no intent tolimit the scope of the present disclosure to the specific embodimentsdescribed herein.

Generally, the present disclosure is directed to an analyte monitoringsystem comprising a sensor operatively in contact with an analyte to bemonitored, a transmitter operatively coupled to the sensor and areceiver for receiving data information from the transmitter relating tothe concentration or amount of the analyte. The transmitter, which isoperatively coupled to the sensor receives the raw data signals andprocesses the signals into a data packet. Each data packet comprisesthree values, the current analyte value and the two immediatelypreceding analyte values. The data packet is transmitted to a receivercomponent, which is configured to issue an alert when at least twoconsecutive data packets are missed or otherwise not received from thetransmitter.

The receiver includes a display unit for displaying the analyte amountor concentration (e.g., mg/dL) to a user. In this regard, the term“user” includes but is not limited to the actual subject beingmonitored. For example, it is contemplated that the “user” could be acaretaker for the monitored subject. The analyte monitoring system iscapable of continuously or intermittently monitoring an analyte in abiological fluid. In this regard, the biological fluid can be blood,interstitial fluid, urine or another fluid containing the analyte to bemonitored.

The analyte monitoring system is configured to provide a user thecapability to selectively disenable an alarm notification of theoccurrence of an event for a predetermined period of time andselectively re-enable the alarm prior to elapse of the predeterminedperiod of time. In certain embodiments, the event which triggers analarm output notification can include, for example, analyte events, dataloss events and system events.

In one embodiment, the analyte monitoring system is a continuous glucosemonitoring system. In this regard, the analyte events are glucose eventsand include but are not limited to low glucose levels (e.g., when singleor continuous glucose level is below a threshold), high glucose levels(e.g, when a single or continuous glucose level is above a threshold),decreasing glucose trend or increasing glucose trend. For the purpose ofillustration, there are multiple ways to configure an analyte monitoringsystem to output an alarm notification based on an increasing ordecreasing glucose trend. For example, the trend information can bebased on multiple glucose datapoints in which the rate of changeindicates a trend, or alternatively, a projected trend information canbe based on predicting or projecting that the glucose level will exceeda particular threshold value based on a current trend.

Data loss events include but are not limited to a disconnection betweenthe receiver and transmitter, improper insertion or implantation of thesensor, expired calibration, sensor error (e.g., not being able tocalculate glucose), transmitter error (e.g., high work current noise,persistent skin temperature out of range, etc), or receiver error (e.g.,RF data packet timing synchronization between CGE and UI processor waslost). System events include but are not limited to battery status(e.g., one week of battery remains, replacement battery needed), failedcalibration, calibration request, early signal attenuation, accelerationof most recent valid data is too large, high signal saturation detectedby transmitter, sensitivity is too high or too low, outlier detected,lost preferences, RF connection has been down for a predetermined timeperiod (e.g., five minutes), log data corrupted, detected insertiontransient, and sensor removal.

FIG. 1 illustrates an analyte monitoring system 100 of the presentdisclosure. As shown in FIG. 1, the analyte monitoring system 100includes sensor 101 operatively coupled to a transmitter unit 102. Thetransmitter unit is in operative communication with a primary receiver104 via communication path 103. In certain embodiments, the analytemonitoring system can further include a secondary receiver 106. Incertain embodiments, each of the receivers 104, 106 may be configured totransmit data information to a remote processor 105.

In certain embodiments, the sensor 101 of the analyte monitoring system100 includes a substrate, a working electrode, a counter electrode, anda reference electrode. The working electrode, the counter electrode andthe reference electrode are formed from conductive material. Examplesinclude, but are not limited to, gold, carbon, Ag/Cl, and the like. Inone embodiment, the substrate and electrodes are arranged in a stackedorientation, such as when insulating material is disposed between theelectrodes.

A sensing layer, which includes at least one immobilized enzyme and animmobilized mediator agent is disposed on at least a portion of at leastthe working electrode. In one embodiment, the immobilized molecule isglucose oxidase and the mediator agent includes a noble metal, such asbut not limited to osmium. The sensor can further include abiocompatible layer. The biocompatible layer is disposed on at least aportion of the sensing layer. In one embodiment, the biocompatiblemembrane and the sensing layer are partially bonded to define aheterogeneous multilayer.

In certain embodiments, the sensor 101 is in operative contact with ananalyte. The term “analyte” refers to a substance or chemicalconstituent in a biological fluid, such as for example, blood orinterstitial fluid. For example and not limitation, the analyte can beglucose, lactate, acetyl choline, amylase, bilirubin, cholesterol,chorionic gonadotropin, creatine kinase (e.g., CK-MB), creatine, DNA,fructosamine, glucose, glutamine, growth hormones, hormones, ketones,peroxide, prostate-specific antigen, prothrombin, RNA, thyroidstimulating hormone, and troponin. However, other analytes can bemonitored as would be understood by one of ordinary skill in the art.

In some embodiments, sensor 101 is implantable into a subject's body fora period of time (e.g., three to five days) to contact and monitor ananalyte present in a biological fluid. In this regard, the sensor can bedisposed in a subject at a variety of sites, including intramuscularly,transcutaneously, intravascularly, or in a body cavity. Sensor 101 isconfigured to generate data signals relative to the amount orconcentration of the analyte to be monitored.

Sensor 101 operatively contacts the analyte to be measured and generatesraw data signals relating to the amount or concentration of the analytedetected. In certain embodiments, transmitter 102 is operatively coupledto sensor 101 and obtains information relating to the data signals fromsensor 101. The transmitter 102 processes the data signals (e.g.,encodes signals) received from the sensor 101 into a data packet. Thedata packet comprises a current analyte value and the two immediatelypreceding analyte values. The data packets are transmitted to receiver104 via radiofrequency communications link 103.

In one embodiment, the transmitter 102 also includes a temperaturesensor. In this regard, the temperature sensor measures an ambienttemperature of the system. Alternatively, the transmitter can beconfigured to be worn on the skin of a user. Thus, the temperaturesensor measures the skin temperature of the user.

The analyte monitoring system 100 also includes a receiver 104, whichaccepts analyte values from the transmitter over a communication link103. Communication link 103 may be a wired communication link or awireless communication link utilizing protocols including, but notlimited to, radio frequency (RF), radio frequency identification (RFID),infrared (IR) or Bluetooth® communication protocols. In certainembodiments, the receiver 104 comprises an input device for receivinguser input, a processor, and a computer readable medium for storing datarelating to the operation of the analyte monitoring device and software,which when executed by the processor, determines whether an alertcondition exists, whether the alert is disenabled or whether a datapacket from the transmitter is not received or otherwise missed by thereceiver. Thus, the receiver is configured to expect a data packet andissue an alert when an expected data packet is not received.Furthermore, the receiver may also include a memory that is capable oflogging analyte concentration or analyte amount values. The receiver 104may also allow a user to erase the logged analyte concentration oramount values.

As will be discussed in further detail below, the receiver 104 isconfigured to expect a data packet from the transmitter 102 atpredetermined time intervals, such as, for example, every five minutesor less. In another embodiment, the receiver 104 is configured to expecta data packet from the transmitter 102 every minute or less. Still yetother embodiments provide that the user may select how often thereceiver 104 should expect a data packet from the transmitter 102.Additionally, it is contemplated that data packets may be expected bythe receiver 104 at different times depending on a condition of theuser. For example, when a critical event or semi-critical event isdetected, the receiver 104 may expect data packets more frequently thanwhen continuous glucose readings are more stable.

In certain embodiments, the receiver 104 alerts the user to reconnectthe receiver or the transmitter if a predetermined number of consecutivedata packets are not received by the receiver 104. For example, if threeconsecutive data packets are not received by the receiver, an alert isissued. The alert can be an auditory alert, a visual alert, a tactilealert, or a combination thereof. Still yet other embodiments providethat the alert can be a continuous alert if the receiver fails toreceive more than five consecutive data packets from the transmitter.The analyte monitoring system can be configured to automaticallydisengage an alert notifying a user of non-receipt of data packets uponthe subsequent receipt of a data packet.

The receiver 104 uses the data to compute an analyte concentration oramount. The receiver 104 can be configured to display glucose values. Inone embodiment, the receiver 104 includes two interconnected centralprocessors. In one embodiment, one central processor is configured fordisplaying images on a display screen such as an LCD screen, user inputand output functionality, as well as handling the user-interface of thereceiver 104. The second central processor may be configured for teststrip measurements, such as calibration, radiofrequency link radiointerface, and a real time clock.

As discussed above, the receiver 104 also includes a display fordisplaying an indication of the level of the measured analyte as well asnotifications of alerts. In one embodiment, the display unit may beseparate from the receiver. In the alternative, the display unit can becoupled to the receiver. In some embodiments, the receiver and/ordisplay unit may include a variety of components, such as, for example,a transmitter, an analyzer, a data storage unit, a watchdog circuit, aninput device, a power supply, a clock, a lamp, a pager, a telephoneinterface, a computer interface, an alarm or alarm system, a radio, anda calibration unit. In some embodiments, the receiver 104 provides adisplay screen for a line graph that plots logged analyte values versustime.

FIG. 2 is a flowchart illustrating a method for detecting a missed datapacket and issuing an alert in accordance with one embodiment of thepresent disclosure. As discussed above, a receiver, such as receiver 104of the analyte monitoring system 100 of FIG. 1, may be configured toexpect a data packet from a transmitter, such as transmitter 102(FIG. 1) at regular time intervals. In certain embodiments, the timeintervals may be every five minutes. In alternative embodiments, thetime interval may be every minute. Still yet other embodiments providethat the interval may automatically change based on a detected conditionof a user, a time of day, or a user initiated event, such as, forexample, exercising, eating a meal, etc. Regardless of the time intervalused, the receiver may be configured to anticipate a data packet at theselected or predetermined time interval.

Accordingly, in certain embodiments, as shown in FIG. 2, a processor ofthe receiver 104 is configured to determine whether data packets arereceived from the transmitter 102 at predetermined time intervals. Incertain embodiments, the predetermined time intervals may be userselectable. In other embodiments, the predetermined time intervals arebased on a monitored condition of a user. For example, if a rate ofchange of an analyte level of the user is within a predeterminedthreshold, the predetermined time interval may be three minutes. If therate of change of the user's analyte level exceeds the threshold, thepredetermined time interval may be one minute. If the processordetermines that the receiver 104 has not received a data packet asexpected (210) the receiver may be configured to attempt to recapturedata packets automatically, requiring no user intervention. For example,the receiver 104 may issue a command to the transmitter 102 requestingthat the transmitter 102 resend the last data packet. When the requestis received, the transmitter 102 resends the last data packet via thecommunication link 103. If the processor detects that a single expecteddata packet was not received, the processor does not issue a command togenerate an alert and the processor resumes detecting an arrival of asubsequent data packet.

If however, the processor detects that a first predetermined number(220) (e.g., two) of consecutive expected data packets were not receivedby the receiver 104, the processor issues a command to generate an alertnotification (230). In certain embodiments, the alert notification maybe a single alert or a series of alerts. Additionally, the alertnotification may be an icon displayed on a display screen of the device,flashing lights, a warning screen and the like. Alternatively, the alertnotification may be an auditory notification or a vibratory notificationor a combination thereof.

In certain embodiments, the type of alert notifications may be userselectable. Additionally, the alerts may be color coded or havedifferent volumes or vibration speeds based on a severity of the alertcondition. For example, if the notification is a warning screen havingtext, the color of the text, a border of the screen or a background oftext may be color coded based on number of consecutive data packetsmissed. In certain embodiments where the alert is an auditory alert, thetone and/or volume of the auditory alert may be user selectable. Forexample, if two data packets in a row were missed, two low volume beepsmay sound. If however, three data packets in a row are missed, thevolume may change to medium level and three beeps may sound. Inembodiments, a user may select a tone, the length of the tone and thevolume of the tone for each auditory notification. Finally, if the alertis a vibratory alert, the user may select the duration and/or frequencyof the vibration.

Referring back to FIG. 2, once the alert is issued, the receiver 104 isconfigured to wait for a predetermined time interval, such as, forexample, one minute, before checking the receipt of the next expecteddata packet. Although a one minute time interval is specificallymentioned, it is contemplated that the predetermined time interval maybe more or less than one minute.

In certain embodiments, the predetermined time interval mayautomatically adjust based on the severity of the alert, such as, forexample, the number of consecutive data packets not received. Thus, thehigher the number of consecutive data packets not received, the smallerthe predetermined time interval. Alternatively, the predetermined timeinterval may correspond to the interval at which the data packets areexpected to arrive at the receiver 104. Thus, if data packets areexpected to arrive at the receiver 104 every two minutes, thepredetermined time interval is two minutes. Still yet other embodimentsprovide that the predetermined time interval corresponds to a fractionof time of the expected data packet arrival at the receiver 104. Thus,if a data packet is expected every five minutes, the predetermined timeis two and a half minutes or some other fraction of time.

If the first predetermined number of consecutive data packets has notbeen received and there has been no user action to remedy the loss ofthe data packets, the processor of the receiver 104 detects whether asecond predetermined amount of consecutive data packets has not beenreceived. In certain embodiments, the count of consecutive data packetsnot received is not reset until at least one data packet is received.Other embodiments provide that the count of the number of consecutivedata packets not received is reset by the processor after an alarm isacknowledged. If it is determined that a second predetermined number ofconsecutive data packets has not been received (240), the processorissues a command to generate a secondary alert (250) to notify the userto reconnect the receiver 104 and/or transmitter 102. For example, iffive consecutive data packet are not received, an alert can be issued,by enabling an “RF MISSED A FEW” message or any other message orindication to indicate multiple data packets have been missed. Asdiscussed above, the alert may be auditory, visual tactile or acombination thereof. If a user does not respond to the alert after apredetermined amount of time, the receiver 104 waits for a predeterminedamount (280) of time before determining whether a subsequent data packetis received. In certain embodiments, because a second predeterminednumber of consecutive data packets were not received, the predeterminedamount of time (280) may be reduced accordingly. For example, if fiveconsecutive data packets were missed, the predetermined amount of timemay be reduced from two minutes to one minute. Thus, as the number ofconsecutive data packets that are missed increases, the predeterminedamount of time before checking the receipt of the next expected datapacket is reduced.

If the processor of the receiver 104 detects a third predeterminednumber of consecutive expected data packets are not received by thereceiver (260), the processor of the receiver 104 is configured to issuean alert (270), such as, for example, a persistent alarm that notifiesthe user to reconnect the receiver 104 to the transmitter 102. Incertain embodiments, the persistent alert may not be mutable. Otherembodiments provide that a user may silence or “snooze” the alert for asmall amount of time. However, once the time period expires, the alertis triggered again. Other embodiments provide that if the alert issilenced repeatedly, the ability to silence the alarm is deactivated.Still yet other embodiments provide that the volume of the alertincrease after each time the alert is snoozed or silenced. In certainembodiments, when the third predetermined number of consecutive alertshas been reached or exceeded, other alert notifications may be inactive.If the alert condition is not addressed by the user within a specifiedamount of time, the receiver 104 waits for the predetermined amount oftime (280) before checking the receipt of the next expected data packet.If a data packet is not received, the alert is triggered.

In certain embodiments, regardless of how many consecutive data packetshave been missed, the receiver 104 can be configured to de-assert (290)any issued alert after it successfully receives the next expected datapacket subsequent to one or consecutive missed data packets. It will berecognized by one skilled in the art that the receiver can be configuredto issue an alert and de-assert an alert based on a different number ofconsecutive missed data packets. For example, if five consecutive datapackets have been missed and an alert has been issued, the receiver maybe configured to de-assert the alert only when a predetermined number ofconsecutive data packets (e.g., three) have been received withoutinterruption.

As discussed above, the alert issued by the receiver may contain one ormore individual alarms. In one embodiment, the alert is a tri-modalalarm, which includes a visual notification (e.g., icon, message, orflashing lights), tactile notification (e.g. vibration) and audible(e.g., beep or ring tones, or music). Other sensory-stimulating alarmsystems may be used including alerts which heat, cool, or produce a mildelectrical shock when triggered.

In another aspect, the analyte monitoring system 100 (FIG. 1) includesan alarm notification feature to alert or warn a user of an event, suchas, for example, a critical event like a potentially detrimentalcondition. For example, if glucose is the analyte, the alarm may notifya user of hypoglycemia, hyperglycemia, impending hypoglycemia, and/orimpending hyperglycemia. In this regard, the alarm is configured suchthat when the data from the sensor 101 reaches or exceeds a thresholdvalue, it outputs an alarm notification. Some non-limiting examples ofthreshold values for blood glucose levels are about 60, 70, or 80 mg/dLfor hypoglycemia, about 70, 80, or 90 mg/dL for impending hypoglycemia,about 130, 150, 175, 200, 225, 250, or 275 mg/dL for impendinghyperglycemia, and about 150, 175, 200, 225, 250, 275, or 300 mg/dL forhyperglycemia.

The threshold values that are designed into the alarm can correspond tointerstitial fluid glucose concentrations or electrode measurements(e.g., current values or voltage values obtained by conversion ofcurrent measurements) that correlate to the above-mentioned bloodglucose levels. The analyte monitor system may be configured so that thethreshold levels for these or any other conditions may be programmableby the patient, caregiver or medical professional.

In certain embodiments, a threshold value is exceeded if a datapoint,such as a glucose datapoint, has a value that is above or below thethreshold value indicating an impending or particular condition, such ashypoglycemia or hyperglycemia. For the purpose of illustration, adatapoint correlating to a glucose level of 200 mg/dL exceeds thethreshold value (180 mg/dL) for hyperglycemia, and indicates that themonitored subject has already entered a hyperglycemic state. As anotherexample, a datapoint correlating to a glucose level of 65 mg/dL exceedsa threshold value (70 mg/dL) for hypoglycemia and indicates that themonitored subject entered a hypoglycemic state. However, a datapointcorrelating to a glucose level of 75 mg/dL would not exceed the samethreshold value for hypoglycemia because the datapoint does not indicatea hypoglycemic state as defined by the predetermined threshold value.

The analyte monitoring system can also be configured to activate analarm, such as by embedded software, if the sensor readings indicatethat a value is beyond a measurement range of the sensor 101. Forglucose, the physiologically relevant measurement range is typicallyabout 50 to 250 mg/dL, preferably about 40 to 300 mg/dL and ideally 30to 400 mg/dL, of glucose in the interstitial fluid. The alarm may also,or alternatively, be activated when the rate of change or accelerationof the rate of change in the analyte level increases or decreases at orabove a predetermined threshold rate or acceleration. For example, inthe case of a subcutaneous glucose monitor, the alarm system might beactivated if the rate of change in glucose concentration exceeds athreshold value which might indicate that a hyperglycemic orhypoglycemic condition is likely to occur.

The alarm may be configured to output a notification if a single datapoint meets or exceeds a particular threshold value. Alternatively, thealarm may be configured to output a notification if a predeterminednumber of datapoints spanning a predetermined amount of time meet orexceed the threshold value. As another alternative, an alarmnotification may be output only when the datapoints spanning apredetermined amount of time have an average value which meets orexceeds the threshold value. Each condition that can trigger an alarmmay have a different alarm activation condition. In addition, the alarmactivation condition may change depending on current conditions (e.g.,an indication of impending hyperglycemia may alter the number ofdatapoints or the amount of time that is tested to determinehyperglycemia).

FIG. 3 is a flowchart illustrating a concurrent passive notificationroutine in a receiver of the analyte monitoring system according to oneembodiment of the present disclosure. In certain embodiments, theanalyte monitoring system, such as the analyte monitoring system 100 ofFIG. 1, can include a concurrent passive notification routine. At thestart of the concurrent passive notification routine, a processor of thereceiver 104 (FIG. 1) executes a predetermined routine (310) for a timeperiod until the routine is completed. Such routines may include bloodglucose tests, calibration routines, medication dosage adjustments, suchas a bolus dose or an update to a basal regiment. Other embodimentsprovide that the routine is a user initiated routine such as viewingvarious display screens on the receiver, updating system preferences,manually entering data such as, for example, event data, and the like.During the execution of the predetermined routine, an alarm condition isdetected (320) by the processor of the receiver 104. In certainembodiments, the alarm condition may be triggered by a datapointexceeding a threshold. When the alarm condition is detected, theprocessor causes a first indication associated with the detected alarmcondition to be output concurrent with the execution of thepredetermined routine (330).

In accordance with one embodiment, when the predetermined routine isbeing executed and an alarm condition is detected, a notificationassociated with the detected alarm condition is provided to the userwithout disrupting the routine. In certain embodiments, the alarmnotification may be an audible beep or noise, a backlight indicator, anicon, a modification in any display item feature such as a border arounda field that flashes, or a text output on the user interface display orany other suitable output indication to alert the user of the detectedalarm condition substantially in real time, but which does not disruptthe ongoing routine. For example, when the predetermined routine isbeing executed, an icon or other visual indicator may be displayed in acorner of the current display screen of the predetermined routine toindicate that an alarm condition is detected.

Upon termination of the predetermined routine (340), another output orsecond indication associated with the detected alarm condition is outputor displayed. In certain embodiments, the processor of the receiver 104may detect that the predetermined routine has terminated andsubsequently output the second indication. For example, if thepredetermined routine is a calibration routine, the processor detectswhen the calibration is complete. In other embodiments, such as, forexample, user initiated routines, the termination of the routine may bedetermined or detected based on a user activated event via the userinterface. In certain embodiments, the second indication associated withthe detected alarm condition is sounded and/or displayed moreprominently. For example, and as described above, as the predeterminedroutine is executing, the alarm may be a soft tone or sound, adiscretely displayed icon or textual message, a slight color change tothe background of the current display screen and the like. However, whenthe routine is finished executing, the alarm is sounded or displayedprominently to indicate the detection of the alert condition.

In a further aspect, the user interface notification feature associatedwith the detected alarm condition is output to the user only upon thecompletion of an ongoing routine which was in the process of beingexecuted when the alarm condition was detected.

In another aspect, the receiver is configured to provide a user thecapability to disenable the alarm notification output for apredetermined time period and to re-enable the alarm notification priorto termination of the predetermined time period. Thus, if the user isrunning a routine or a series of routines that will take a substantialamount of time, the user may select to disenable the output of the firstalarm and/or the output of the second alarm for a predetermined amountof time. In one embodiment, a glucose monitoring system is configured toallow the user to disenable an alarm notification, via a user interface,only if the user's blood glucose level is within predeterminedparameters, such as for example, between about 60 and 139 mg/dL.

As discussed above, the alarm may contain one or more individual alarms.In one embodiment, the alarm is a tri-modal alarm, which includes avisual notification (e.g., icon or flashing lights), tactilenotification (e.g. vibration) and audible (e.g., beep or ring tones, ormusic). Other sensory-stimulating alarm systems may be used includingalarms which heat, cool, or produce a mild electrical shock whentriggered. In some embodiments, auditory alarms have different tone,note, or volume indicating different conditions. For example, a highnote might indicate hyperglycemia and a low note might indicatehypoglycemia. Visual alarms may use a difference in color, brightness toindicate different conditions or severity levels. In some embodiments,an auditory alarm is configured so that the volume of the alarmincreases over time until the alarm is deactivated.

In some embodiments, the alarm may be automatically deactivated after apredetermined time period. In other embodiments, the alarm may beconfigured to deactivate when the data no longer indicates that thecondition which triggered the alarm exists. In these embodiments, thealarm may be deactivated when a single data point indicates that thecondition no longer exists or, alternatively, the alarm may bedeactivated only after a predetermined number of datapoints or anaverage of the datapoints obtained over a given period of time indicatethat the condition no longer exists.

Other embodiments provide that the alarm may be deactivated manually bya user. In these embodiments, a switch is provided and when actuated,the alarm is turned off. The switch may be operatively engaged (ordisengaged depending on the configuration of the switch) by, forexample, operating an actuator on sensor 101 or the receiver/displayunit 104. In some cases, an actuator may be provided on two or moreunits including the sensor 101, transmitter 102, primary receiver 104,secondary receiver 106, or elsewhere, any of which may be actuated todeactivate the alarm.

A variety of switches may be used including, for example, a mechanicalswitch, a reed switch, a Hall effect switch, a Gigantic Magnetic Ratio(GMR) switch (the resistance of the GMR switch is magnetic fielddependent) and the like. Preferably, the actuator used to operativelyengage (or disengage) the switch is placed on the sensor 101 andconfigured so that no water can flow around the button and into thehousing. One example of such a button is a flexible conducting stripthat is completely covered by a flexible polymeric or plastic coatingintegral to the housing. In an open position the flexible conductingstrip is bowed and bulges away from the housing. When depressed by thepatient or another person, the flexible conducting strip is pusheddirectly toward a metal contact and completes the circuit to shut offthe alarm.

In instances when a reed or GMR switch is used, a flexible actuatorcontaining a magnetic material, such as a permanent magnet or anelectromagnet may be used to deactivate the alarm. In such embodiments,the flexible actuator may bulge away from the housing. Thus, when reedor GMR switch is activated (to deactivate the alarm) by depressing theflexible actuator, the magnetic material is brought closer to the switchwhich causes an increase in the magnetic field within the switch and thealarm is deactivated.

FIG. 4 is a flowchart illustrating an alarm notification disenabling andre-enabling routine in a receiver of the analyte monitoring system inaccordance with one embodiment of the present disclosure. In certainembodiments and as described below, the analyte monitoring system 100(FIG. 1) provides a user with the capability to disenable the alarmprior to activation of an alarm notification by a particular event, suchas a single data point exceeding a threshold, a hyperglycemic state, adecreasing trend of analyte concentrations. In this regard, a user canaccess the alarms menu to disenable and re-enable the alarm from a userinterface of analyte monitoring system.

The routine for disenabling and re-enabling alarm notifications beginswhen a user is presented with a user interface on a receiver 104(FIG. 1) and the user makes a selection of one of the options thereon(410). In certain embodiments, the user interface includes a main menuhaving a plurality of selection options. Nonlimiting examples of theselection options may include “Glucose,” “Alarms,” “Reports,” “System,”and “Add Event.” A user may navigate the list of options and select oneof the options using an actuator disposed on the receiver 104, such as,for example, a jog wheel, arrow keys on the receiver, a touch sensitiveportion of the display and the like. When a processor of the receiver104 detects user selection of the “Alarms” option, a submenu for the“Alarms” option is displayed (420). In certain embodiments, the submenuof the “Alarms” option that includes an alarm menu for disenablingand/or muting alarms is displayed only if the alarm notification is notalready disenabled (for example audible alarm muted). Alternatively, thesubmenu user interface that includes an alarm menu for disenablingand/or muting alarms is displayed regardless of whether alarmnotifications are disenabled. Still yet other embodiments provide thatselection of the submenu will only display alarms that can be muted ordisenabled.

When the mute alarm option is selected from user menu the receiverdisplays a user interface that allows a user to select a predeterminedperiod of time for disenablement or muting of the alarm notification(430). In embodiments, user selection is enabled using an actuatordisposed on the receiver 104. Selectable predetermined periods can betwelve or less hours. Further, the predetermined time for more than onehour can be by hourly increments. In still yet further embodiments, whena user desires to re-enable the alarm notification, the user interfaceof the receiver 104 provides a display screen with the option tore-enable the alarm notification feature. In this regard, the userinterface provides a menu selection to enable the user to un-mute thealarm notification (440). In certain embodiments, the user interface foralarm re-enablement only shows alarms which have been previouslydisenabled and/or muted.

If desired, the display screen of receiver 104 is configured to blankthe user interface if no selection is made in a predetermined period oftime. For example, the receiver 104 can be configured to blank or fadeto black within twenty or more seconds if no selection is made. Otherembodiments provide that if a user selection is not made in apredetermined time period, the user is returned to the main menu screen.

In one embodiment, an icon is displayed on the receiver display toindicate alarms are disenabled and/or muted. In some embodiments, theuser is allowed to turn off low and high glucose alarms only if the userturns off each alarm mode individually.

FIG. 5 is a flowchart illustrating a method for detecting an alertcondition in accordance with one embodiment of the present disclosure.At the start of the routine, a processor of the receiver 104 (FIG. 1)detects an alert condition (510). In embodiments, the alert conditionmay be detected because of a critical event such as a low glucose levelof a user, a decreasing blood glucose trend of the user, a hypoglycemicevent, or a blood glucose level above or below a particular thresholdlevel. In other embodiments, the detected alert condition may correspondto non-critical such as, for example, low battery status or low sensorlife.

When an alert condition is detected, the processor determines whether aroutine is currently being executed (520). Such routines may includeblood glucose tests, calibration routines, and medication dosageadjustments, such as a bolus dose or an update to a basal regiment.Other embodiments provide that the routine is a user initiated routinesuch as viewing various display screens on the receiver 104, updatingsystem preferences, or manually entering data into the receiver.

If the processor determines that a routine is not currently beingexecuted, such as, for example, by detecting an idle state of thereceiver, the processor issues a command to generate a primary alertnotification (570). In one embodiment, the alert notification mayinclude a visual notification (e.g., icon, message, or flashing lights),a tactile notification (e.g. vibration), an audible notification (e.g.,beep or ring tones, or music) or a combination thereof.

If the processor determines that a routine is currently being executed,the processor of the receiver 104 issues a command to generate asecondary alert notification (530). In embodiments, the secondary alertnotification is displayed or otherwise activated so as to not disruptthe routine that is currently being executed. Thus, in certainembodiments, the alarm notification may be an audible beep or noise, abacklight indicator, an icon, a modification in any display item featuresuch as a border around a field that flashes, or a text output on theuser interface display that may be output substantially simultaneouslywith the routine.

After the secondary alert is generated by the processor, the processordetermines whether the condition that triggered the alarm is stillpresent (540). For example, if a low battery triggered the alertcondition, the processor determines whether the battery has beenrecharged or is currently recharging. If the alert condition wastriggered because a blood glucose level was above or below a particularthreshold, the processor determines whether a recent blood glucose levelreading is within the predetermined threshold. If it is determined thatthe condition that triggered the alert no longer exists, the processorissues a command to deactivate the alarm (560).

If however, it is determined that the condition that triggered the alertstill exists, the processor once again determines whether the routine iscurrently being executed (520). If it is determined that the routine isno longer being executed, the processor issues a command to trigger theprimary alert notification (570) as described above. However, if it isdetermined that the routine is no longer being executed and thecondition that triggered the alert no longer exists, the processorissues a command to deactivate any alarms that may still be active.

The various embodiments of detecting missed data packets, issuingalerts, and disenabling and enabling the alerts can be implemented inthe receiver which comprises a processor, and a computer readable mediumfor storing data relating to the operation of the analyte monitoringdevice and software, which when executed by the processor, determineswhether a data packet from the transmitter is not received, or otherwisemissed by the receiver, and whether to issue an alert to the user. Thus,the receiver is configured to expect a data packet and issue an alertwhen an expected data packet is not received.

In one embodiment, an analyte monitoring system includes a sensor inoperative contact with an analyte, the sensor adapted to generate a datasignal associated with an amount or concentration of the analyte; atransmitter operatively coupled to the sensor and adapted to process theraw data signal generated by the sensor to define a data packet, whereinthe data packet comprises a current analyte value and the previous twoanalyte values; and a receiver operatively linked to the transmitter andcapable of receiving the data packet from the transmitter, wherein thereceiver is configured to alert a user if at least two consecutive datapackets are not received by the receiver.

In another embodiment, the receiver receives the data packet from thetransmitter via a radio-frequency communications link.

Further embodiments provide that the alert is a visual alert such as,for example, an icon.

In an embodiment, the alert is an audible alert such as a beep, a toneor music.

In still yet other embodiments, the alert is a tactile alert such as,for example, a vibration of a component of the analyte monitoringsystem.

Embodiments also include configurations where the receiver alerts theuser to reconnect the receiver or the transmitter if more than twoconsecutive data packets are not received by the receiver.

In certain embodiments, the receiver is configured to expect a datapacket from the transmitter every five minutes or less or every minuteor less.

In one aspect, the alert automatically disengages when a data packet isreceived by the receiver subsequent to non-receipt of an earlier datapacket.

In another aspect, the alert is a continuous alert if the receiver failsto receive more than five consecutive data packets from the transmitter.

In certain embodiments, the analyte is glucose, and the analytemonitoring system is a continuous glucose monitoring system.

Still yet other embodiments provide that the receiver is wirelesslylinked to a data management host.

In other embodiments, the sensor comprises a substrate, a workingelectrode, a counter electrode, and a reference electrode arranged in astacked orientation, and further wherein each of the electrodes isformed from a conductive material.

In another embodiment an analyte monitoring system includes a sensor inoperative contact with an analyte, the sensor adapted to generate a datasignal associated with an amount or concentration of the analyte; atransmitter coupled to the sensor and adapted to process the data signalgenerated by the sensor; and a receiver capable of receiving theprocessed data signal and outputting an alarm notification based on anevent, wherein the receiver is configured to allow a user to disenablethe alarm notification for a predetermined time period and to re-enablethe alarm notification prior to elapse of the predetermined time period.

In one embodiment, the alarm is a tri-modal alarm and includes anaudible alarm, a visual alarm and a tactile alarm.

In yet another embodiment, the receiver is adapted to disenable only onemode of the alarm.

In one aspect, the disenabled alarm notification is muting an audiblealarm.

In another aspect, the predetermined time is about one to twelve hours.

In yet another aspect, the predetermined period is more than one hourand further the mute is set in one hour increments for the entirepredetermined period.

Embodiments provide that the receiver is capable of displaying an iconindicator when the alarm is muted.

Other embodiments provide that the alarm is incapable of beingdisenabled by a user for a critical event such as, for example, a lowglucose event.

In one embodiment, the event is a system or data loss event.

Still yet other embodiments provide that the sensor further includesinsulating material disposed between the electrodes.

Embodiments also provide that a sensing layer is disposed on at least aportion of at least the working electrode, the sensing layer includingat least one immobilized enzyme and an immobilized mediator agent.

In certain embodiments, the sensor further includes a biocompatiblemembrane disposed on at least a portion of the sensing layer.

Embodiments provide that the biocompatible membrane is at leastpartially bonded to the sensing layer to define a heterogeneousmultilayer.

In an embodiment, the transmitter is worn on the body of a user.

In an embodiment, the transmitter is a temperature sensor.

Embodiments also provide that the receiver has a memory capable logginganalyte concentration or amount values.

Still further embodiments provide that the receiver is configured toallow a user to erase the logged analyte concentration or amount values.

Various other modifications and alterations in the structure and methodof operation of this disclosure will be apparent to those skilled in theart without departing from the scope and spirit of the embodiments ofthe present disclosure. Although the present disclosure has beendescribed in connection with particular embodiments, it should beunderstood that the present disclosure as claimed should not be undulylimited to such particular embodiments. It is intended that thefollowing claims define the scope of the present disclosure and thatstructures and methods within the scope of these claims and theirequivalents be covered thereby.

What is claimed is:
 1. A method, comprising: establishing a communication link between a sensor electronics and a data receiver, the communication link configured for transmission of data packets between the sensor electronics and the data receiver; determining that a first level of data packets received by the data receiver from the sensor electronics is less than a first threshold; providing an alert associated with a severity based on the first level and the first threshold; waiting for a time interval based on the severity; after the time interval, determining that a second level of data packets received by the data receiver from the sensor electronics is less than a second threshold; and generating a persistent secondary alert based on the second level and the second threshold.
 2. The method of claim 1, wherein the communication link is according to at least one of a radio frequency protocol, a radio frequency identification protocol, an infrared protocol, or a Bluetooth communication protocol.
 3. The method of claim 1, wherein the first threshold corresponds to a first count of unreceived consecutive data packets, and the second threshold corresponds to a second count of unreceived consecutive data packets.
 4. The method of claim 1, wherein the secondary alert includes at least one of an unmutable auditory component or a visual component.
 5. The method of claim 1, wherein the secondary alert includes a notification to a user to reconnect the sensor electronics and the data receiver.
 6. The method of claim 1, wherein the sensor electronics is operatively coupled to an in vivo sensor which comprises a plurality of electrodes including a working electrode comprising an analyte-responsive enzyme bonded to a polymer disposed on the working electrode.
 7. The method of claim 6, wherein the analyte-responsive enzyme is chemically bonded to the polymer.
 8. The method of claim 6, wherein the working electrode further comprises a mediator.
 9. The method of claim 1, wherein the sensor electronics is operatively coupled to an in vivo sensor which comprises a plurality of electrodes including a working electrode comprising a mediator bonded to a polymer disposed on the working electrode.
 10. The method of claim 9, wherein the mediator is chemically bonded to the polymer.
 11. A system, comprising: a sensor electronics operatively coupled to an in vivo analyte sensor; and a data receiver, the data receiver configured to: establish a communication link with the sensor electronics, the communication link configured for transmission of data packets between the sensor electronics and the data receiver; determine that a first level of data packets received from the sensor electronics is less than a first threshold; provide an alert associated with a severity based on the first level and the first threshold; wait for a time interval based on the severity; after the time interval, determine that a second level of data packets received from the sensor electronics is less than a second threshold; and generate a persistent secondary alert based on the second level and the second threshold.
 12. The system of claim 11, wherein the communication link is according to at least one of a radio frequency protocol, a radio frequency identification protocol, an infrared protocol, or a Bluetooth communication protocol.
 13. The system of claim 11, wherein the first threshold corresponds to a first count of unreceived consecutive data packets, and the second threshold corresponds to a second count of unreceived consecutive data packets.
 14. The system of claim 11, wherein the secondary alert includes at least one of an unmutable auditory component or a visual component.
 15. The system of claim 11, wherein the secondary alert includes a notification to a user to reconnect the sensor electronics and the data receiver.
 16. The system of claim 11, wherein the in vivo sensor comprises a plurality of electrodes including a working electrode comprising an analyte-responsive enzyme bonded to a polymer disposed on the working electrode.
 17. The system of claim 16, wherein the analyte-responsive enzyme is chemically bonded to the polymer.
 18. The system of claim 16, wherein the working electrode further comprises a mediator.
 19. The system of claim 11, wherein the in vivo sensor which comprises a plurality of electrodes including a working electrode comprising a mediator bonded to a polymer disposed on the working electrode.
 20. The system of claim 19, wherein the mediator is chemically bonded to the polymer. 